Canonical Allele Identifier: CA344043425

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197403899T>C (hg19) ; chr1:g.197434769T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197434769T>C , CM000663.2:g.197434769T>C	GRCh38
NC_000001.10:g.197403899T>C , CM000663.1:g.197403899T>C	GRCh37
NC_000001.9:g.195670522T>C	NCBI36
NG_008483.1:g.171492T>C
NG_008483.2:g.238308T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2906T>C MANE Select	ENSP00000356370.3:p.Ile969Thr
ENST00000638467.1:c.2906T>C	ENSP00000491102.1:p.Ile969Thr
ENST00000681519.1:c.1787T>C	ENSP00000505267.1:p.Ile596Thr
ENST00000367397.1:c.1049T>C	ENSP00000356367.1:p.Ile350Thr
ENST00000367399.6:c.2570T>C	ENSP00000356369.2:p.Ile857Thr
ENST00000367400.7:c.2906T>C	ENSP00000356370.3:p.Ile969Thr
ENST00000484075.5:c.2906T>C	ENSP00000433932.1:p.Ile969Thr
ENST00000535699.5:c.2834T>C	ENSP00000438786.1:p.Ile945Thr
ENST00000538660.5:c.2129-831T>C	ENSP00000438091.1:n.2129-831T>C
NM_001193640.1:c.2570T>C	NP_001180569.1:p.Ile857Thr
NM_001257965.1:c.2834T>C	NP_001244894.1:p.Ile945Thr
NM_001257966.1:c.2129-831T>C	NP_001244895.1:n.2129-831T>C
NM_201253.2:c.2906T>C	NP_957705.1:p.Ile969Thr
NR_047563.1:n.2907T>C
NR_047564.1:n.3115T>C
XM_011509365.1:c.2906T>C	XP_011507667.1:p.Ile969Thr
XM_011509366.1:c.2906T>C	XP_011507668.1:p.Ile969Thr
XM_011509367.1:c.2906T>C	XP_011507669.1:p.Ile969Thr
XM_011509368.1:c.2324T>C	XP_011507670.1:p.Ile775Thr
XM_011509369.1:c.1349T>C	XP_011507671.1:p.Ile450Thr
XM_011509365.2:c.2906T>C	XP_011507667.1:p.Ile969Thr
XM_011509369.2:c.1349T>C	XP_011507671.1:p.Ile450Thr
XM_017000851.1:c.2063T>C	XP_016856340.1:p.Ile688Thr
XM_017000852.1:c.3041T>C	XP_016856341.1:p.Ile1014Thr
NM_201253.3:c.2906T>C MANE Select	NP_957705.1:p.Ile969Thr
NM_001193640.2:c.2570T>C	NP_001180569.1:p.Ile857Thr
NM_001257965.2:c.2834T>C	NP_001244894.1:p.Ile945Thr
NR_047563.2:n.2859T>C
NR_047564.2:n.3067T>C
NM_001257966.2:c.2129-831T>C	NP_001244895.1:n.2129-831T>C